PDE3A mutations cause autosomal dominant hypertension with brachydactyly.

Maass, Philipp G

PDE3A mutations cause autosomal dominant hypertension with brachydactyly. [electronic resource] - Nature genetics Jun 2015 - 647-53 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.

1546-1718

10.1038/ng.3302 doi


Adolescent
Adult
Amino Acid Sequence
Animals
Base Sequence
Brachydactyly--genetics
Case-Control Studies
Cell Differentiation
Child
Cyclic Nucleotide Phosphodiesterases, Type 3--genetics
Female
Genetic Association Studies
HeLa Cells
Humans
Hypertension--congenital
Kinetics
Male
Mesenchymal Stem Cells--physiology
Mice
Middle Aged
Molecular Sequence Data
Mutation, Missense
Myocytes, Smooth Muscle--physiology
Pedigree